Package 43063-943-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-943-30
Digits Only 4306394330
Product NDC 43063-943
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-943-30)

Marketing

Marketing Status
Marketed Since 2018-01-31
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415eeebb-cc6b-0538-e063-6394a90a1ac9", "openfda": {"upc": ["0343063943304"], "unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["4789b7ae-314c-43c0-ad33-92ff50085f27"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-943-30)", "package_ndc": "43063-943-30", "marketing_start_date": "20180131"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "43063-943_415eeebb-cc6b-0538-e063-6394a90a1ac9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "43063-943", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040786", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}